HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2-Dimethyl-3-(toluene-4-sulfonyloxy)butyric acid methyl ester → 2,2-Dimethyl-3-butenoic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2-Dimethyl-3-(toluene-4-sulfonyloxy)butyric acid methyl ester | HCID 21031493 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Product | 2,2-Dimethyl-3-butenoic acid methyl ester | HCID 11693910 | 130% |
Reaction Steps
A solution of 2,2-dimethyl-3-(toluene-4-sulfonyloxy)butyric acid methyl ester (18.06 g, 0.06 mol) in DBU (15 ml) was heated at 140-160° for 3.5 h. The mixture was allowed to cool to room temperature and was then diluted with ether. The mixture was washed with HCl (1 M), sodium bicarbonate, then brine. The ethereal layer was dried and partially evaporated to give a concentrated solution of 2,2-dimethyl-but-3-enoic acid methyl ester (10 g). (Savu and Katzenellenbogen, J Org. Chem, 46:239-250 (1981)). Further evaporation was avoided due to the volatility of the product (bp 102°). (Tsaconas et al., Aust. J Chem., 53:435-437 (2000)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07919497B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-6832993b02824294830665895908bcaf |
| Source note | uspto-grants-2011_04 |